A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893102



Internal ID18837236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:50871431..50953868hg38UCSC Ensembl
Outerchr18:50871431..50953868hg38UCSC Ensembl
Innerchr18:48397801..48480238hg19UCSC Ensembl
Outerchr18:48397801..48480238hg19UCSC Ensembl
Innerchr18:46651799..46734236hg18UCSC Ensembl
Outerchr18:46651799..46734236hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3882438
hg1982438
hg1882438
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786806
Samples
Known GenesME2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893102
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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